Succinylcholine Chloride
- Product NDC
- 70518-4409
- 11-digit product format
- 705184409
- Labeler code
- 70518
- Product ID
- 70518-4409_3b144826-0fef-8a7c-e063-6394a90ad55b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211589
- Marketing category
- ANDA
- Marketing start
- 2025-07-29
- Substance
- SUCCINYLCHOLINE CHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Succinylcholine Chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUCCINYLCHOLINE CHLORIDE | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I9L0DDD30I |
| Rxcui | 1594589 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4409-0 | Succinylcholine Chloride | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 1 |
| 70518-4409-1 | Succinylcholine Chloride | 10 mL in 1 VIAL | INJECTION, SOLUTION | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4409-0 | 70518440900 | 10 VIAL in 1 CARTON (70518-4409-0) / 10 mL in 1 VIAL (70518-4409-1) | 10 vial | 2025-07-29 | No | No | Current |
| 70518-4409-1 | 70518440901 | 10 mL in 1 VIAL | 10 ml | | | | Historical |